HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → N-(5-Cyclohexyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazole | HCID 53924444 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-Cyclohexyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamide | HCID 21454603 | — |
Reaction Steps
A solution of methylhydrazine (0.3 mole) in methylene chloride (150 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 5-cyclohexyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.1 mole) is then added, with stirring, at room temperature. After the addition is completed the reaction mixture is heated at reflux for a period of about 4 hours. After this time the reaction mixture is stripped of solvent and excess hydrazine to yield the desired product 2-methyl-4-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)semicarbazide as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007031 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-319a862fa58843e28fc753fafe5e3f6e |
| Source note | uspto-grants-1977_02 |